JPH03207798A - Cleanser composition - Google Patents

Cleanser composition

Info

Publication number
JPH03207798A
JPH03207798A JP422390A JP422390A JPH03207798A JP H03207798 A JPH03207798 A JP H03207798A JP 422390 A JP422390 A JP 422390A JP 422390 A JP422390 A JP 422390A JP H03207798 A JPH03207798 A JP H03207798A
Authority
JP
Japan
Prior art keywords
amino
modified silicone
weight
surfactant
acyl group
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP422390A
Other languages
Japanese (ja)
Other versions
JPH06102797B2 (en
Inventor
Hideji Tagata
秀次 田方
Tomoko Nihei
二瓶 智子
Fumio Sai
崔 文雄
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kao Corp
Original Assignee
Kao Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kao Corp filed Critical Kao Corp
Priority to JP2004223A priority Critical patent/JPH06102797B2/en
Publication of JPH03207798A publication Critical patent/JPH03207798A/en
Publication of JPH06102797B2 publication Critical patent/JPH06102797B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
    • C11D3/3742Nitrogen containing silicones

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)

Abstract

PURPOSE:To provide a light cleanser composition having an excellent felt shrinkage-preventing property for garments by compounding a surfactant and a specific amino-modified silicone amide in a specified ratio. CONSTITUTION:The objective composition contains (A) 5-70wt.% (preferably 10-40wt.%) of a surfactant preferably consisting of an alkylbenzene sulfonate salt, alkylether sulfate salt, olefin sulfonate salt, alkane sulfonate salt or polyoxyethylene alkyl(phenyl) ether and (B) 0.05-5wt.% (preferably 0.1-3wt.%) of an amino-modified silicone amide compound having a 7-24C acyl group (which may have a polyoxyethylene chain therein) at the N terminal of the amino- modified silicone as a substituent.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は洗浄剤組底物に関し、更に詳しくは衣類の縮み
防止性(フエルト収縮防止性)に優れた軽質の洗浄剤組
底物に関する. 〔従来の技術及びその課題〕 ウール製品、絹製品等の繊細な衣料は、生地を傷めない
ように軽質の洗剤を使用して手洗いであるいは弱い機械
力をかけて洗濯されている.しかし、これらの衣料中で
も特にウール製品はぬるま湯中で軽くもみ洗い又は押し
洗いする等の細心の注意を払ってもなお縮む傾向(フエ
ルト収縮)があることは日常よく経験するところである
. 先に、本発明者らはカチオン性基又は三級アミノ基を有
する粒径がo.oos〜0.2−の微細な高分子ラテッ
クスを配合した軽質洗剤がフエルト収縮防止に著しい効
果があることを見出した(特開昭63 − 8492号
公報、特開昭63 − 89596号公報)。しかしな
がら、このような微細な高分子ラテックスの製造は特殊
な製造条件を必要とするなど、工業的に不利な面があっ
た.〔課題を解決するための手段〕 本発明者らは高分子ラテックスに代わる基剤について鋭
意研究した結果、ある種のシリコーン化合物を配合した
洗浄剤が優れたフェルト収縮防止効果を奏する曇とを見
出し本発明を完或するに至った. すなわち本発明は、 (a)  界面活性剤        5〜70重量%
(b)アミノ変性シリコーン中の末端窒素原子に炭素数
7〜24のアシル蟇(アシル基鎖中にポリオキシエチレ
ン鎖を有していてもよい)が置換基として結合してなる
アミノ変性シリコーンアξド化物 0.05〜5重量% を含有してなる洗浄剤組威物を提供するものである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a detergent assembly, and more particularly to a lightweight detergent assembly with excellent clothing shrinkage prevention properties (felt shrinkage prevention properties). [Prior art and its problems] Delicate clothing such as wool products and silk products are washed by hand using light detergents or by applying weak mechanical force to avoid damaging the fabric. However, it is a common daily experience that among these types of clothing, wool products in particular have a tendency to shrink (felt shrinkage) even when careful care is taken, such as gently rubbing or washing them in lukewarm water. First, the present inventors discovered that particles having a cationic group or a tertiary amino group have a particle size of o. It has been found that a light detergent containing a fine polymer latex with a particle size of 0.00 to 0.2 is extremely effective in preventing felt shrinkage (Japanese Unexamined Patent Publication Nos. 8492-1984 and 89596-1983). However, manufacturing such fine polymer latex requires special manufacturing conditions, which is industrially disadvantageous. [Means for Solving the Problem] As a result of intensive research into base materials that can replace polymer latex, the present inventors have discovered that a cleaning agent containing a certain type of silicone compound has an excellent effect of preventing felt shrinkage. The present invention has now been completed. That is, the present invention includes (a) surfactant 5 to 70% by weight
(b) An amino-modified silicone in which an acyl group having 7 to 24 carbon atoms (which may have a polyoxyethylene chain in the acyl group chain) is bonded to the terminal nitrogen atom of the amino-modified silicone as a substituent. The present invention provides a detergent composition containing 0.05 to 5% by weight of ξdide.

本発明に洗浄主基剤として使用される界面活性剤(a)
は、従来一般に使用されている疎水基の炭素数が8〜2
4を有するものでよく、例えば陰イオン性界面活性剤と
しては、直鎖又は分岐鎖アルキルベンゼンスルホン酸塩
、アルキル又はアルケニルエーテル硫酸塩、アルキル又
はアルケニル硫酸塩、オレフィンスルホン酸塩、アルカ
ンスルホン酸塩、α−スルホ脂肪酸塩又はエステル、飽
和又は不飽和脂肪酸塩、アルキル又はアルケニルエーテ
ルカルポン酸塩、アミノ酸型界面活性剤、N−アシルア
ミノ酸型界面活性剤、アルキル又はアルケニル燐酸エス
テル又はその塩等が例示される. また、両性界面活性剤としては、カルボキシ又はスルホ
ベタイン型界面活性剤等が、非イオン性界面活性剤とし
ては、ポリオキシアルキレンアルキル又はアルケニルエ
ーテル、ポリオキシエチレンアルキルフェニルエーテル
、高級脂肪酸アルカノールアミド又はそのアルキレンオ
キサイド付加物、蔗糖脂肪酸エステル、脂肪酸エステル
、脂肪酸グリセリンモノエステル、アルキルアミンオキ
サイド等が例示される.これらの界面活性剤の中でも特
にアルキルベンゼンスルホン酸塩、アルキルエーテル硫
酸塩、オレフィンスルホン酸塩、アルカンスルホン酸塩
、ポリオキシエチレンアルキルエーテル、ポリオキシエ
チレンアルキルフェニルエーテルが好適である。
Surfactant (a) used as main cleaning base in the present invention
The conventionally commonly used hydrophobic group has 8 to 2 carbon atoms.
For example, anionic surfactants include linear or branched alkylbenzene sulfonates, alkyl or alkenyl ether sulfates, alkyl or alkenyl sulfates, olefin sulfonates, alkanesulfonates, Examples include α-sulfo fatty acid salts or esters, saturated or unsaturated fatty acid salts, alkyl or alkenyl ether carponates, amino acid type surfactants, N-acylamino acid type surfactants, alkyl or alkenyl phosphate esters or their salts, etc. It will be done. Examples of amphoteric surfactants include carboxy or sulfobetaine type surfactants, and examples of nonionic surfactants include polyoxyalkylene alkyl or alkenyl ethers, polyoxyethylene alkylphenyl ethers, higher fatty acid alkanolamides, and the like. Examples include alkylene oxide adducts, sucrose fatty acid esters, fatty acid esters, fatty acid glycerin monoesters, and alkylamine oxides. Among these surfactants, alkylbenzene sulfonates, alkyl ether sulfates, olefin sulfonates, alkanesulfonates, polyoxyethylene alkyl ethers, and polyoxyethylene alkylphenyl ethers are particularly preferred.

界面活性剤は通常洗浄剤組威物中に5〜70重量%、好
ましくは10〜40重量%配合される。
The surfactant is usually incorporated in the detergent composition in an amount of 5 to 70% by weight, preferably 10 to 40% by weight.

本発明に用いられる(b)或分はアミノ変性シリコーン
中の窒素原子に結合する水素原子が、炭素数7〜24の
アシル碁(アシル基鎖中にポリオキシエチレン鎖を有し
ていてもよい)で厘摸された構造を有するアミノ変性シ
リコーンア竜ド化物である。アシル基の炭素数が7未満
の場合には十分なフェルト収縮防止効果が得られない。
The hydrogen atom bonded to the nitrogen atom in (b) or the amino-modified silicone used in the present invention is an acyl group having 7 to 24 carbon atoms (which may have a polyoxyethylene chain in the acyl group chain). ) is an amino-modified silicone aridide having a structure simulated by When the number of carbon atoms in the acyl group is less than 7, a sufficient effect of preventing felt shrinkage cannot be obtained.

かかるアミノ変性シリコーンアミド化物としては下記一
般式(1)で表される化合物が好ましく、特にアシル基
鎖中に1〜30モル、好ましくは1〜10モルのポリオ
キシエチレン鎖を有するものが少量で優れた効果を奏す
るので望ましい.〔式中、 R :炭素数1〜4のアルキル基、ヒドロキシ基、アル
コヰシ基 Rl:炭素数1〜4のアルキル基であり、それぞれ異な
っていてもよい A : Rχ t −(Cut)m−N−8 又は であり、ここで a,b;2〜6、好ましくは2〜3の整数Rt,RS 
*水素原子又は炭素数1〜4のアルキル碁を示す B  ;  C  (CHz)c(CJ−0)t  R
a11 0 であり、ここで c ;1〜6、好ましくは2〜4の整数d :0〜30
、好ましくは1〜30、特に好ましくは1〜10の整数 R4:炭素数6〜18のアルキル基 を示す.〕 上記一般式(1)で表されるシリコーン化合物の分子量
は2000〜150000、アミン当量は1000〜2
0000の範囲が好ましく、園,nはこれらに対応する
数である. 伽)威分は組或物中に0.05〜5重量%、好ましくは
0.1〜3重量%配合される. 尚、従来ジメチルポリシロキサンに代表されるシリコー
ン化合物は泡調節剤として一般番ご汎用されている。ま
た、特開昭60−215099号公報にはアξノ変性シ
リコーン又はその誘導体を洗剤に少量配合することによ
り衣類に柔軟性を付与できることが記載されている.し
かしながら、本発明で使用するアミノ変性シリコーンア
ミド化物は従来洗剤系中で使用されているこれらのシリ
コーン化合物とはその構造及び作用効果の両者において
異なるものである。
As such amino-modified silicone amidated products, compounds represented by the following general formula (1) are preferred, and in particular those having 1 to 30 moles, preferably 1 to 10 moles of polyoxyethylene chains in the acyl group chain are preferred. It is desirable because it has excellent effects. [In the formula, R: an alkyl group having 1 to 4 carbon atoms, a hydroxy group, an alkoxy group Rl: an alkyl group having 1 to 4 carbon atoms, each of which may be different A: Rχ t -(Cut)m-N -8 or, where a, b; integers Rt, RS of 2 to 6, preferably 2 to 3;
*B indicating a hydrogen atom or an alkyl having 1 to 4 carbon atoms; C (CHz)c(CJ-0)t R
a110, where c; an integer of 1 to 6, preferably 2 to 4 d: 0 to 30
, preferably from 1 to 30, particularly preferably from 1 to 10. Integer R4: represents an alkyl group having 6 to 18 carbon atoms. ] The molecular weight of the silicone compound represented by the above general formula (1) is 2000 to 150000, and the amine equivalent is 1000 to 2.
A range of 0000 is preferable, and 0 and n are numbers corresponding to these.佽)Ibun is blended in the composition in an amount of 0.05 to 5% by weight, preferably 0.1 to 3% by weight. Incidentally, silicone compounds typified by dimethylpolysiloxane have conventionally been commonly used as foam control agents. Furthermore, JP-A No. 60-215099 describes that flexibility can be imparted to clothing by incorporating a small amount of ξ-anomodified silicone or its derivatives into detergent. However, the amino-modified silicone amides used in the present invention are different from these silicone compounds conventionally used in detergent systems both in structure and effect.

本発明組戒物の残部は水、芒硝等のフィラーであるが、
この種の軽質洗剤に配合される他の任意威分を配合する
ことができる。このような任意威分として、ポリアクリ
ル酸、ポリビニルピロリドン、ポリエチレングリコール
、カルボキシメチルセルロース等の再汚染防止剤:ブロ
テアーゼ、アもラーゼ、リバーゼ、セルラーゼ等の酵素
;塩化カルシウム等の酵素安定化剤:エタノール等の低
級アルコール:ベンゼンスルホン酸塩、P−}ルエンス
ルホン酸塩等の低級アルキルベンゼンスルホン酸塩;プ
ロピレングリコール等のグリコール類;安息香酸塩、尿
素等の可溶化剤;t−プチルヒドロキシトルエン、ジス
チレン化クレゾール等の酸化防止剤;その他蛍光染料、
青味付剤、香料、抗菌剤等が挙げられる。
The remainder of the composition of the present invention is fillers such as water and mirabilite.
Other optional ingredients that are included in this type of light detergent may be included. Such optional agents include recontamination preventive agents such as polyacrylic acid, polyvinylpyrrolidone, polyethylene glycol, and carboxymethyl cellulose; enzymes such as protease, amolase, reverse, and cellulase; enzyme stabilizers such as calcium chloride; and ethanol. Lower alcohols such as benzenesulfonates, P-}luenesulfonates, and other lower alkylbenzenesulfonates; Glycols such as propylene glycol; Benzoates, solubilizers such as urea; t-butylated hydroxytoluene, distyrene Antioxidants such as cresol; other fluorescent dyes,
Examples include blue tinting agents, fragrances, antibacterial agents, and the like.

また、本発明組或物は通常の洗剤ビルダー或分を実質上
含まないことが望ましいが、ジグリコール酸塩、リン酸
塩、炭酸塩等のビルダー或分を2〜3重量%以下であれ
ば配合することもできる。
Further, it is desirable that the composition of the present invention does not substantially contain any ordinary detergent builders, but if it contains no more than 2 to 3% by weight of builders such as diglycolates, phosphates, carbonates, etc. It can also be blended.

〔実 施 例〕〔Example〕

以下実施例にて本発明を説明するが、本発明はこれらに
限定されるものではない。
The present invention will be explained below with reference to Examples, but the present invention is not limited thereto.

実施例1 第1表に示す各種洗浄剤組或物を調製し、以下の方法に
よりフェルト収縮率及び面積収縮率を測定した。
Example 1 Various cleaning compositions shown in Table 1 were prepared, and the felt shrinkage rate and area shrinkage rate were measured by the following methods.

〔I〕フェルト収縮率及び面積収縮率の測定(1)供試
布の調製 三方をロックミシンでかがった、大きさ10X IOC
I1のウールの未加工布を、常温の水道水に30分間浸
漬後、脱水槽にて30秒間脱水し、綱の上に載せて平干
しし、20゜C165%RHで4時間以上調湿した。こ
の布に油性のサインペンで4カ所印を付け、それぞれに
番号を付した後、それぞれの印の間の長さを測定し(タ
テalO+a!’ *ヨコb,’, bz’)、この長
さを原長とした. (2)洗濯方法 ターグー0−}メーター(Terg−0−Tomete
r.上島製作所製)を用い、(1)で得た供試布3枚を
1つのポットに入れ、120 r.p.va.で10分
間回転させて洗濯を行った.各洗剤濃度は0.25重量
%とし、水温は20℃とした.すすぎとしては、一回目
はポット中の流水すすぎ、二回目は手洗い桶中の流水す
すぎを行った.次いで、この供試布を洗濯機の脱水槽の
壁につけて30秒間脱水後、網の上にのせて平干しして
乾燥させ、20″C、65%RHで4時間以上調湿した
[I] Measurement of felt shrinkage rate and area shrinkage rate (1) Preparation of sample fabric Sewn on three sides with lock sewing machine, size 10X IOC
The unprocessed wool cloth of I1 was immersed in tap water at room temperature for 30 minutes, dehydrated for 30 seconds in a dehydration tank, placed on a rope to dry flat, and conditioned at 20°C and 165% RH for over 4 hours. . Mark 4 places on this cloth with an oil-based felt-tip pen, number each one, then measure the length between each mark (vertical alO+a!' * horizontal b,', bz'), and find this length. is the original length. (2) Washing method Terg-0-Tomete
r. (manufactured by Ueshima Seisakusho), the three test fabrics obtained in (1) were placed in one pot, and heated at 120 r.m. p. va. I washed it by spinning it for 10 minutes. The concentration of each detergent was 0.25% by weight, and the water temperature was 20°C. For rinsing, the first rinse was done with running water in a pot, and the second time was with running water in a hand washing tub. Next, this sample fabric was applied to the wall of the dehydration tank of a washing machine to dehydrate it for 30 seconds, then placed on a net to dry flat, and the humidity was controlled at 20''C and 65% RH for over 4 hours.

更に、先に(1)で付した印について再度それらの間の
長さを測定し(タテal’+ a!W ;ヨコb,’,
 bz’) 、これから次式に従ってフエルト収縮率を
算出し、それより面積収縮率を算出した.この結果を第
1表に示す。
Furthermore, the length between the marks made in (1) was measured again (vertical al'+ a!W; horizontal b,',
bz') From this, the felt shrinkage rate was calculated according to the following formula, and the area shrinkage rate was calculated from it. The results are shown in Table 1.

く収縮率の真出(I賀ST門より)〉 R.M. :洗濯前の測定[(原長) W.M. :洗濯後の測定値 〈面積収縮率の算出〉 W.S.X L.S. 面積収縮率(%) −Jl.S.+L.S.− 100 W.S. :横方向のフエルト収縮率 L.S. :縦方向のフエルト収縮率 分子量14000, ア壽ン当量4670 シリコーン(2): 一般式(I) において : CI’[, A : (CHz) s ?H−(CH.)■一NH C−CxJss 11 0 分子量7000、 アξン当量3500 シリコーン(3); 一般式(1) において :CH, : − (CHz) s−Nil (CD!) t−NH−C−CJq 11 0 分子量6000、 アミン当量3000 高分子ラテックス: n−プチルアクリレート/ジエチルアミノエチルメタク
リレー}−95/5、 重量平均 径0.07m、 ガラス転移点 219° K
True determination of shrinkage rate (from Iga ST gate) R. M. : Measurement before washing [(original length) W. M. : Measured value after washing (calculation of area shrinkage rate) W. S. XL. S. Area shrinkage (%) -Jl. S. +L. S. - 100 W. S. : Horizontal felt shrinkage rate L. S. : vertical felt shrinkage molecular weight 14000, silicone equivalent 4670 Silicone (2): In general formula (I): CI'[, A: (CHz) s? H-(CH.)■-NH C-CxJss 11 0 Molecular weight 7000, Aξ equivalent weight 3500 Silicone (3); In general formula (1): CH, : - (CHz) s-Nil (CD!) t- NH-C-CJq 110 Molecular weight 6000, Amine equivalent 3000 Polymer latex: n-butyl acrylate/diethylaminoethyl methacrylate}-95/5, Weight average diameter 0.07 m, Glass transition point 219°K

Claims (1)

【特許請求の範囲】 1(a)界面活性剤5〜70重量% (b)アミノ変性シリコーン中の末端窒素原子に炭素数
7〜24のアシル基(アシル基鎖中にポリオキシエチレ
ン鎖を有していてもよい)が置換基として結合してなる
アミノ変性シリコーンアミド化物 0.05〜5重量% を含有してなる洗浄剤組成物。
[Scope of Claims] 1 (a) 5 to 70% by weight of surfactant (b) An acyl group having 7 to 24 carbon atoms (having a polyoxyethylene chain in the acyl group chain) at the terminal nitrogen atom in the amino-modified silicone. A cleaning composition comprising 0.05 to 5% by weight of an amino-modified silicone amidated compound having an amino-modified silicone amide bonded thereto as a substituent.
JP2004223A 1990-01-10 1990-01-10 Cleaning composition Expired - Lifetime JPH06102797B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2004223A JPH06102797B2 (en) 1990-01-10 1990-01-10 Cleaning composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2004223A JPH06102797B2 (en) 1990-01-10 1990-01-10 Cleaning composition

Publications (2)

Publication Number Publication Date
JPH03207798A true JPH03207798A (en) 1991-09-11
JPH06102797B2 JPH06102797B2 (en) 1994-12-14

Family

ID=11578595

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2004223A Expired - Lifetime JPH06102797B2 (en) 1990-01-10 1990-01-10 Cleaning composition

Country Status (1)

Country Link
JP (1) JPH06102797B2 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07242897A (en) * 1994-03-04 1995-09-19 Nippon Oil & Fats Co Ltd Liquid detergent composition
JPH0967594A (en) * 1995-09-01 1997-03-11 Kao Corp Detergent composition
JPH115903A (en) * 1997-04-21 1999-01-12 Toray Dow Corning Silicone Co Ltd Composition of organopolysiloxane modified with polyoxyethylene alkyl ether fatty acid amide
JPH115904A (en) * 1997-04-21 1999-01-12 Toray Dow Corning Silicone Co Ltd Surface modifier composition
JP2013213171A (en) * 2012-04-04 2013-10-17 Asahi Kasei Chemicals Corp New silicone derivative

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5035119A (en) * 1973-07-31 1975-04-03
JPS60215099A (en) * 1984-01-25 1985-10-28 ザ、プロクタ−、エンド、ギヤンブル、カンパニ− Liquid detergent compositon containing organic functional polysiloxane
JPS62133177A (en) * 1985-11-25 1987-06-16 ダウ・コ−ニング・コ−ポレ−シヨン Method for washing fabric

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5035119A (en) * 1973-07-31 1975-04-03
JPS60215099A (en) * 1984-01-25 1985-10-28 ザ、プロクタ−、エンド、ギヤンブル、カンパニ− Liquid detergent compositon containing organic functional polysiloxane
JPS62133177A (en) * 1985-11-25 1987-06-16 ダウ・コ−ニング・コ−ポレ−シヨン Method for washing fabric

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07242897A (en) * 1994-03-04 1995-09-19 Nippon Oil & Fats Co Ltd Liquid detergent composition
JPH0967594A (en) * 1995-09-01 1997-03-11 Kao Corp Detergent composition
JPH115903A (en) * 1997-04-21 1999-01-12 Toray Dow Corning Silicone Co Ltd Composition of organopolysiloxane modified with polyoxyethylene alkyl ether fatty acid amide
JPH115904A (en) * 1997-04-21 1999-01-12 Toray Dow Corning Silicone Co Ltd Surface modifier composition
JP2013213171A (en) * 2012-04-04 2013-10-17 Asahi Kasei Chemicals Corp New silicone derivative

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